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  1. Article

    Open Access

    JAK2 as a surface marker for enrichment of human pluripotent stem cells-derived ventricular cardiomyocytes

    Human pluripotent stem cell (hPSC)-derived cardiomyocytes (CMs) hold great promise for cardiac disease modelling, drug discovery and regenerative medicine. Despite the advancement in various differentiation pr...

    Lee Chuen Liew, Boon Min Poh, Omer An, Beatrice Xuan Ho in Stem Cell Research & Therapy (2023)

  2. Article

    Open Access

    Robust generation of human-chambered cardiac organoids from pluripotent stem cells for improved modelling of cardiovascular diseases

    Tissue organoids generated from human pluripotent stem cells are valuable tools for disease modelling and to understand developmental processes. While recent progress in human cardiac organoids revealed the ab...

    Beatrice Xuan Ho, Jeremy Kah Sheng Pang, Ying Chen in Stem Cell Research & Therapy (2022)

  3. Article

    Correction: PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP production

    Upadhyayula S. Srinivas, Norbert S. C. Tay, Patrick Jaynes, Akshaya Anbuselvan in Oncogene (2022)

  4. Article

    Open Access

    Pan-cancer pervasive upregulation of 3′ UTR splicing drives tumourigenesis

    Most mammalian genes generate messenger RNAs with variable untranslated regions (UTRs) that are important post-transcriptional regulators. In cancer, shortening at 3′ UTR ends via alternative polyadenylation c...

    Jia Jia Chan, Bin Zhang, **ao Hong Chew, Adil Salhi, Zhi Hao Kwok in Nature Cell Biology (2022)

  5. Article

    Open Access

    Multilayered control of splicing regulatory networks by DAP3 leads to widespread alternative splicing changes in cancer

    The dynamic regulation of alternative splicing requires coordinated participation of multiple RNA binding proteins (RBPs). Aberrant splicing caused by dysregulation of splicing regulatory RBPs is implicated in...

    Jian Han, Omer An, ** Ren, Yangyang Song, Sze **g Tang in Nature Communications (2022)

  6. No Access

    Article

    p53-NEIL1 co-abnormalities induce genomic instability and promote synthetic lethality with Chk1 inhibition in multiple myeloma having concomitant 17p13(del) and 1q21(gain)

    Recurrent cytogenetic abnormalities are the main hallmark of multiple myeloma (MM) and patients having 2 or more high-risk prognostic events are associated with extremely poor outcome. 17p13(del) and 1q21(gain...

    Phaik Ju Teoh, Omer An, Tae-Hoon Chung, Thamil Vaiyapuri, Anandhkumar Raju in Oncogene (2022)

  7. Article

    Open Access

    ADARs act as potent regulators of circular transcriptome in cancer

    Circular RNAs (circRNAs) are produced by head-to-tail back-splicing which is mainly facilitated by base-pairing of reverse complementary matches (RCMs) in circRNA flanking introns. Adenosine deaminases acting ...

    Haoqing Shen, Omer An, ** Ren, Yangyang Song, Sze **g Tang in Nature Communications (2022)

  8. No Access

    Article

    PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP production

    Inhibitors of the mitotic kinase PLK1 yield objective responses in a subset of refractory cancers. However, PLK1 overexpression in cancer does not correlate with drug sensitivity, and the clinical development ...

    Upadhyayula S. Srinivas, Norbert S. C. Tay, Patrick Jaynes, Akshaya Anbuselvan in Oncogene (2022)

  9. Article

    Open Access

    Cis- and trans-regulations of pre-mRNA splicing by RNA editing enzymes influence cancer development

    RNA editing and splicing are the two major processes that dynamically regulate human transcriptome diversity. Despite growing evidence of crosstalk between RNA editing enzymes (mainly ADAR1) and splicing machi...

    Sze **g Tang, Haoqing Shen, Omer An, HuiQi Hong, Jia Li in Nature Communications (2020)

  10. Article

    Open Access

    Mitochondrial 3243A > G mutation confers pro-atherogenic and pro-inflammatory properties in MELAS iPS derived endothelial cells

    Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a mitochondrial disorder that is commonly caused by the m.3243A > G mutation in the MT-TL1 gene encoding for mitochon...

    Nicole Min Qian Pek, Qian Hua Phua, Beatrice Xuan Ho in Cell Death & Disease (2019)